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nsv6983681

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,278

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 86 SVs from 21 studies. See in: genome view    
    Submitted genomic27,957,616-27,960,893Question Mark
    Overlapping variant regions from other studies: 86 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):26,284,642-26,287,919Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6983681Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1727,957,61627,960,893
    nsv6983681RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1726,284,64226,287,919

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18406239deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18406239Submitted genomicNC_000017.11:g.279
    57616_27960893del
    GRCh38 (hg38)NC_000017.11Chr1727,957,61627,960,893
    nssv18406239RemappedPerfectNC_000017.10:g.262
    84642_26287919del
    GRCh37.p13First PassNC_000017.10Chr1726,284,64226,287,919

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv184062397e-062275990
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